Role & Responsibilities
• Prepare and manage global regulatory submissions (eCTD)
• Handle lifecycle management submissions (CMC, SPL, amendments)
• Coordinate documentation for global health authority filings
• Ensure regulatory compliance and audit readiness
Qualification: B.Pharm / M.Pharm
Experience: 1-3 years
Skills
• Knowledge of regulatory processes and global submissions
• Proficiency in eCTD publishing, Veeva Vault, DocuBridge
• Strong attention to detail and compliance mindset
• Excellent communication and coordination skills
About The Company
• Accenture is a global leader in professional services and life sciences operations.
• The company offers structured growth, global exposure, and compliance-driven roles aligned with international regulatory standards.
• Accenture provides an inclusive and equal-opportunity workplace, working with leading biopharma clients.
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